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dc.contributor.authorHaliloglu, G.
dc.contributor.authorTALİM, BERİL
dc.contributor.authorALİKAŞİFOĞLU, MEHMET
dc.contributor.authorTopaloglu, H.
dc.contributor.authorMARAŞ GENÇ, Hülya
dc.contributor.authorArdicli, D.
dc.date.accessioned2023-10-10T10:22:45Z
dc.date.available2023-10-10T10:22:45Z
dc.identifier.citationMARAŞ GENÇ H., Ardicli D., Haliloglu G., TALİM B., ALİKAŞİFOĞLU M., Topaloglu H., "Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation", 21st International Congress of the World-Muscle-Society, Granada, Nikaragua, 4 - 08 Ekim 2016
dc.identifier.otherav_031dee8a-3766-446a-8399-e861ea57a5d8
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/189210
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2016.06.192
dc.language.isoeng
dc.subjectFizik Bilimleri
dc.subjectYaşam Bilimleri
dc.subjectKLİNİK NÖROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectSİNİR BİLİMİ
dc.subjectSinirbilim ve Davranış
dc.subjectSağlık Bilimleri
dc.subjectTemel Bilimler
dc.subjectDuyusal Sistemler
dc.subjectGelişimsel Sinirbilim
dc.subjectBilişsel Sinirbilim
dc.subjectHücresel ve Moleküler Sinirbilim
dc.subjectSinirbilim (çeşitli)
dc.subjectGenel Sinirbilim
dc.subjectNöroloji (klinik)
dc.subjectİnsan Bilgisayar Etkileşimi
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.titleSolving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutation
dc.typeBildiri
dc.contributor.departmentAnkara Childrens Hematol Oncol Training & Res Hos , ,
dc.contributor.firstauthorID4562303


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